Boron tribromide → 2-(3-Hydroxyphenyl)-2-methylpropanenitrile
反応式
C[O:2][C:3]1[CH:4]=[C:5]([C:9]([CH3:13])([CH3:12])[C:10]#[N:11])[CH:6]=[CH:7][CH:8]=1.B(Br)(Br)Br>C(Cl)Cl>[OH:2][C:3]1[CH:4]=[C:5]([C:9]([CH3:13])([CH3:12])[C:10]#[N:11])[CH:6]=[CH:7][CH:8]=1参加物
4
実験手順
To a stirred solution of 2-(3-methoxyphenyl)-2-methylpropanenitrile (Step A, 4.5 g, 25.7 mmol) in methylene chloride (30 ml) was added BBr3 (1M in CH2Cl2, 50 ml) at −78° C. under argon, the cold bath was substituted by ice bath after 30 minutes and the reaction was stirred at the same temperature for 2 hours and then 30 minutes at room temperature. The reaction mixture was quenched by addition of ice and worked up by washing with water and brine. The organic layer was dried over Na2SO4, filtered, concentrated, and purified by flash chromatography on a silica gel column (methylene chloride:ethyl acetate, 5:1) to give the title compound.